Article ; Online: A mechanistic study of Anwei decoction intervention in a rat model of gastric intestinal metaplasia through the endoplasmic reticulum stress - Autophagy pathway.
2024 Volume 87, Page(s) 102317
Abstract: Objective: To investigate the mechanism of Anwei decoction (AWD) intervention on gastric intestinal metaplasia (GIM) using a rat model through the endoplasmic reticulum stress-autophagy pathway.: Methods: Gastric intestinal metaplasia was induced in ... ...
Abstract | Objective: To investigate the mechanism of Anwei decoction (AWD) intervention on gastric intestinal metaplasia (GIM) using a rat model through the endoplasmic reticulum stress-autophagy pathway. Methods: Gastric intestinal metaplasia was induced in rats using 1-methyl-3-nitro-1-nitrosoguanidine. The experiment included a normal control group, a model group, and low-, medium- and high-dose AWD groups. The specificity of intestinal epithelial cells was determined for model establishment and drug efficacy by detecting the protein expression of markers such as MUC2, VILLIN and CDX2 through western blotting (WB). The effects of AWD on endoplasmic reticulum stress and autophagy were evaluated by measuring the mRNA and protein expression levels of endoplasmic reticulum stress markers (PEPK, ATF6, CHOP and caspase-12) and autophagy markers (LC3Ⅱ and Beclin-1) using reverse transcription polymerase chain reaction and the WB method. Furthermore, the ultrastructure of gastric mucosal cells and autophagosome status were observed using transmission electron microscopy. Results: Compared with the model group, the AWD-treated rats exhibited significant improvement in body weight (P < 0.01), reduced protein expression of the intestine epithelial cell-specific markers MUC2, VILLIN, CDX2 and KLF4 (P < 0.01 for all) and increased SOX2 protein expression (P < 0.01). In addition, AWD suppressed the mRNA and protein expression of endoplasmic reticulum stress markers PEPK and ATF6 (P < 0.01 for all) and promoted the mRNA and protein expression of autophagy and apoptosis markers CHOP, caspase-12, LC3Ⅱ and Beclin-1 (P < 0.01 for all). Conclusion: Anwei decoction effectively inhibits the further progression of GIM and prevents the occurrence of gastric mucosal carcinogenesis. |
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MeSH term(s) | Rats ; Animals ; Signal Transduction ; Beclin-1/genetics ; Beclin-1/pharmacology ; Caspase 12 ; Apoptosis ; RNA, Messenger ; Autophagy ; Endoplasmic Reticulum Stress ; Metaplasia |
Chemical Substances | Beclin-1 ; Caspase 12 (EC 3.4.22.-) ; RNA, Messenger |
Language | English |
Publishing date | 2024-02-01 |
Publishing country | Scotland |
Document type | Journal Article |
ZDB-ID | 204424-9 |
ISSN | 1532-3072 ; 0040-8166 |
ISSN (online) | 1532-3072 |
ISSN | 0040-8166 |
DOI | 10.1016/j.tice.2024.102317 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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